Determination of Paraquat in Environmental Water by Ionic Liquid-Based Liquid Phase Extraction with Direct Injection for HPLC

被引:11
作者
Sha, Ou [1 ,2 ]
Wang, Yu [2 ]
Chen, Xiao-Bin [3 ]
Chen, Juan [4 ]
Chen, Li [1 ]
机构
[1] Huaihai Inst Technol, Anal & Test Ctr, Jiangsu Marine Resources Dev Res Inst, Lianyungang 222001, Peoples R China
[2] Huaihai Inst Technol, Sch Chem & Chem Engn, Lianyungang 222005, Peoples R China
[3] First Peoples Hosp Lianyungang City, Lianyungang 222005, Peoples R China
[4] Jiangsu Union Tech Inst, Lianyungang TCM Branch, Lianyungang 222006, Peoples R China
关键词
paraquat; ionic liquid; HPLC; aqueous two-phase system; IONIZATION MASS-SPECTROMETRY; SPECTROPHOTOMETRIC DETERMINATION; URINE SAMPLES; CAPILLARY-ELECTROPHORESIS; GAS-CHROMATOGRAPHY; FOOD SAMPLES; OLIVE OIL; DIQUAT; HERBICIDES; ELECTRODE;
D O I
10.1134/S1061934818090083
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple method for the determination of paraquat in environment samples was developed. 1-Ethyl-3-methylimidazolium ethyl sulfate and anhydrous potassium hydrogen phosphate were used to form aqueous two-phase system. The system was applied to the extraction of paraquat and its determination by HPLC. To achieve optimum extraction performance, several experimental parameters, including the type and the amount of salt, the amount of ionic liquid, extraction time, were investigated and optimized. Under the optimal experimental conditions, good linearity was observed in the range of 10-5 x 10(3) ng/mL. The limit of detection was 8 ng/mL along with enrichment factor of 18. The phase behavior of aqueous two-phase system and extraction mechanism were investigated by UV-Vis spectroscopy. The present method was successfully applied to the determination of paraquat in environment samples, and the recovery was in the range of 92.3-95.1%. The results showed that the present method is rapid, feasible and environmentally friendly.
引用
收藏
页码:862 / 868
页数:7
相关论文
共 36 条
[1]  
Albertsson P.A., 1986, PARTITION CELL PARTI
[2]   Determination of diquat and paraquat in olive oil by ion-pair liquid chromatography-electro spray ionization mass spectrometry (MRM) [J].
Aramendía, MA ;
Borau, V ;
Lafont, F ;
Marinas, A ;
Marinas, JM ;
Moreno, JM ;
Porras, JM ;
Urbano, FJ .
FOOD CHEMISTRY, 2006, 97 (01) :181-188
[3]   Herbicide-resistant weed management: focus on glyphosate [J].
Beckie, Hugh J. .
PEST MANAGEMENT SCIENCE, 2011, 67 (09) :1037-1048
[4]   AN ION-EXCHANGE METHOD FOR DETERMINING PARAQUAT RESIDUES IN FOOD CROPS [J].
CALDERBANK, A ;
YUEN, SH .
ANALYST, 1965, 90 (1067) :99-+
[5]   Comparison of silica and porous graphitic carbon as solid-phase extraction materials for the analysis of cationic herbicides in water by liquid chromatography and capillary electrophoresis [J].
Carneiro, MC ;
Puignou, L ;
Galceran, MT .
ANALYTICA CHIMICA ACTA, 2000, 408 (1-2) :263-269
[6]  
CHICHILA TM, 1991, J ASSOC OFF ANA CHEM, V74, P961
[7]   Simple flow injection colorimetric system for determination of paraquat in natural water [J].
Chuntib, Prakit ;
Jakmunee, Jaroon .
TALANTA, 2015, 144 :432-438
[8]   Gas chromatographic-mass spectrometric method for the determination of the herbicides paraquat and diquat in plasma and urine samples [J].
de Almeida, Rafael Menck ;
Yonamine, Mauricio .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 853 (1-2) :260-264
[9]   Evaluation of a Nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry [J].
de Oliveira, UMF ;
Lichtig, J ;
Masini, JC .
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2004, 15 (05) :735-741
[10]   Glyphosate-resistant horseweed (Conyza canadensis) control using glyphosate-, paraquat-, and glufosinate-based herbicide programs [J].
Eubank, Thomas W. ;
Poston, Daniel H. ;
Nandula, Vijay K. ;
Koger, Clifford H. ;
Shaw, David R. ;
Reynolds, Daniel B. .
WEED TECHNOLOGY, 2008, 22 (01) :16-21